Complex I deficiency in Persian multiple sclerosis patients

Multiple sclerosis (MS) is a demyelinating disease of the central nervous system characterized by the morphological hallmarks of inflammation, demyelination and axonal loss. Until now, little attention has been paid to the contribution of mitochondrial respiratory chain enzyme activities to MS. In t...

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Veröffentlicht in:	Journal of the neurological sciences 2006-04, Vol.243 (1), p.65-69
Hauptverfasser:	Kumleh, Hassan H., Riazi, Gholam H., Houshmand, Massoud, Sanati, Mohammad H., Gharagozli, Kourosh, Shafa, Mehdi
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Biological and medical sciences Biopsy Central Nervous System - metabolism Central Nervous System - physiopathology Electron Transport Complex I - deficiency Electron Transport Complex I - genetics Encephalomyopathy Energy Metabolism - genetics Female Humans Immunomodulators Infectious Disease Transmission, Vertical Male Medical sciences Mitochondria - genetics Mitochondria - metabolism Mitochondrial complex I Mitochondrial Diseases - complications Mitochondrial Diseases - genetics Mitochondrial Diseases - metabolism Mitochondrial DNA Multiple sclerosis Multiple Sclerosis - genetics Multiple Sclerosis - metabolism Multiple Sclerosis - physiopathology Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis Muscle, Skeletal - metabolism Muscle, Skeletal - physiopathology NADH, NADPH Oxidoreductases - analysis NADH, NADPH Oxidoreductases - genetics NADH, NADPH Oxidoreductases - metabolism Nerve Degeneration - genetics Nerve Degeneration - metabolism Nerve Degeneration - physiopathology Neurology Neurons - metabolism Neurons - pathology Pharmacology. Drug treatments Spectrophotometry
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